EP2583663A1 - Oil-in-water type emulsion skin cosmetic - Google Patents

Oil-in-water type emulsion skin cosmetic Download PDF

Info

Publication number
EP2583663A1
EP2583663A1 EP11795586.4A EP11795586A EP2583663A1 EP 2583663 A1 EP2583663 A1 EP 2583663A1 EP 11795586 A EP11795586 A EP 11795586A EP 2583663 A1 EP2583663 A1 EP 2583663A1
Authority
EP
European Patent Office
Prior art keywords
acid
skin
iob
salt
ingredient
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
EP11795586.4A
Other languages
German (de)
French (fr)
Other versions
EP2583663A4 (en
EP2583663B1 (en
Inventor
Takayuki Omura
Tomomi Furukawara
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Shiseido Co Ltd
Original Assignee
Shiseido Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Shiseido Co Ltd filed Critical Shiseido Co Ltd
Publication of EP2583663A1 publication Critical patent/EP2583663A1/en
Publication of EP2583663A4 publication Critical patent/EP2583663A4/en
Application granted granted Critical
Publication of EP2583663B1 publication Critical patent/EP2583663B1/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/40Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
    • A61K8/44Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/02Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/04Dispersions; Emulsions
    • A61K8/06Emulsions
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/34Alcohols
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/34Alcohols
    • A61K8/345Alcohols containing more than one hydroxy group
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/37Esters of carboxylic acids
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/46Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur
    • A61K8/466Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur containing sulfonic acid derivatives; Salts
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/81Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • A61K8/817Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a single or double bond to nitrogen or by a heterocyclic ring containing nitrogen; Compositions or derivatives of such polymers, e.g. vinylimidazol, vinylcaprolactame, allylamines (Polyquaternium 6)
    • A61K8/8182Copolymers of vinyl-pyrrolidones. Compositions of derivatives of such polymers
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin
    • A61Q19/08Anti-ageing preparations

Definitions

  • the invention relates to an oil-in-water type emulsion skin cosmetic composition having good texture and stability. More specifically, the invention relates to an oil-in-water type emulsion skin cosmetic composition having light spreadability on skin, no stickiness, lightness, a good feeling as an active ingredient effectively penetrates into the skin (good penetrating feeling), and high stability over time.
  • Glycerin is known as a cosmetic ingredient having a high moisturizing effect and a high skin improving effect such as a high skin roughness reducing effect. To produce such a high skin improving effect significantly, glycerin is often added at a content of 5.0% by mass or more. Particularly, skin cosmetics with high glycerin content can produce high skin improving effect but may have the disadvantage in use that as the content increases, dewy feeling or feeling as an active ingredient penetrates into the skin disappears, and stickiness appears.
  • acrylamide thickeners which are used as cosmetic thickeners, provide good texture such as good compatibility to the skin or good spreadability (see for example Patent Documents 4 and 5).
  • Such acrylamide thickeners are useful as an alternative to carboxyvinyl polymer, xanthan gum, or hydroxyethyl cellulose, which is traditionally used as a cosmetic thickener in many cases.
  • glycerin is added at a high concentration to provide a skin improving effect, a problem also occurs in which good texture of acrylamide thickeners is lost and it becomes impossible to reduce the glycerin-induced stickiness.
  • an oil-in-water type emulsion skin cosmetic composition containing (A) a D-amino acid or a derivative or salt thereof, (B) a homopolymer, a copolymer, or a crosspolymer including, as a constituent unit, one or more selected from 2-acrylamido-2-methylpropanesulfonic acid, acrylic acid, and derivatives thereof, (C) an ester oil with an IOB value of 0.2 to 0.6, and (D) glycerin is compatible to the skin and not sticky during use, and can reliably produce a skin improving effect.
  • an oil-in-water type emulsion skin cosmetic composition that has light spreadability on skin, no stickiness, and a good penetrating feeling when an active ingredient penetrates the skin, provides moisture, and is moist even in a system with a high glycerin content, and also allows glycerin to produce a high skin improving effect.
  • the skin cosmetic composition of the invention essentially contains a D-amino acid or a derivative or salt thereof (ingredient (A), hereinafter also abbreviated as "D-amino acid maternal").
  • D-amino acid or a derivative or salt thereof D-amino acid material
  • D-amino acid material means a D-amino acid, a derivative thereof, a salt thereof, or a mixture thereof.
  • amino acids can exist in L-form or D-form which are optical isomers and natural proteins are composed of L-amino acids bonded together by peptide bonds. It has been considered that except for some cases such as bacterial cell walls, only L-amino acids exist in mammals including human and only L-amino acids are used in living bodies. Conventionally, therefore, academic or industrial focus and research have been dominantly on L-amino acids.
  • Exceptional cases where D-amino acids are used include (1) cases where D-amino acids are used as raw materials for antibiotics to be produced by bacteria and (2) cases where food additives contain a mixture of L- and D-amino acids in order to avoid the cost required to isolate the L-amino acid from the mixture (racemic mixture) containing equal amounts of the Land D-amino acids synthesized chemically.
  • D-aspartic acid which does not occur naturally, increases with age in the ocular lens, brain, or skin, and the relationship between it and the development of cataract or Alzheimer's disease has begun to be discussed ( Tadatoshi Kinouchi et al. "proteins, Nucleic Acids, and Enzymes” (in Japanese) Vol. 50, No. 5 (2005), 453-560 ).
  • D-Asp be used as a molecular marker for detecting skin damage caused by aging or ultraviolet rays.
  • D-amino acids are positively used as biologically active materials.
  • the invention is characterized in that a D-amino acid, which has not been conventionally added to cosmetics, especially skin cosmetics, is added as an essential ingredient.
  • the D-amino acid material (ingredient (A)) used in the invention may be of any type as long as it is in the D-form.
  • the D-amino acid material itself can be effective in improving the skin.
  • examples include D-aspartic acid, which can have an antioxidant effect and a collagen production promoting effect, D-alanine, which can have a laminin 332 production promoting effect and a collagen production promoting effect, D-glutamic acid, which can have a barrier recovery function, a wrinkle formation reducing effect, and a skin roughness reducing effect, D-serine, which can have an ultraviolet damage reducing effect, D-hydroxyproline, which can have a laminin 332 production promoting effect, D-cysteine, which can have an ultraviolet damage reducing effect, D-methionine and D-proline, which can have an ultraviolet damage reducing effect, and D-hydroxyproline, which can have a melanin production inhibiting effect.
  • the D-amino acid material used in the invention may be a synthetic product or a commercially available product.
  • a known method for producing a D-amino acid includes allowing bacterial D-aminoacylase to act on an acylated amino acid to obtain a D-amino acid (see JP-A Hei 11-113592 ).
  • the content of the D-amino acid material in the skin cosmetic composition of the invention is preferably from 0.1 to 5.0% by mass based on the total amount of the cosmetic composition.
  • a homopolymer, a copolymer, or a crosspolymer including, as a constituent unit, one or more selected from 2-acrylamido-2-methylpropanesulfonic acid (hereinafter also abbreviated as "AMPS”), acrylic acid, and derivatives thereof, which is used as the ingredient (B) in the invention.
  • AMPS 2-acrylamido-2-methylpropanesulfonic acid
  • acrylic acid and derivatives thereof
  • Examples of the ingredient (B) used in the invention include a vinylpyrrolidone/2-acrylamido-2-methylpropanesulfonic acid (salt) copolymer, a dimethylacrylamide/2-acrylamido-2-methylpropanesulfonic acid (salt) copolymer, an acrylamide/2-acrylamido-2-methylpropanesulfonic acid copolymer, a methylenebisacrylamide-crosslinked dimethylacrylamide/2-acrylamido-2-methylpropanesulfonic acid crosspolymer, a mixture of polyacrylamide and poly (sodium acrylate), a sodium acrylate/2-acrylamido-2-methylpropanesulfonic acid copolymer, a hydroxyethyl acrylate/2-acrylamido-2-methylpropanesulfonic acid (salt) copolymer, poly(ammonium acrylate), a polyacrylamide/ammonium acrylate copolymer, and an acrylamide/sodium acryl
  • the salt include an alkali metal salt (such as a calcium salt or a magnesium salt), an ammonium salt, and an organic amine salt (such as a monoethanolamine salt, a diethanolamine salt, or a triethanolamine salt).
  • alkali metal salt such as a calcium salt or a magnesium salt
  • ammonium salt such as sodium bicarbonate
  • organic amine salt such as a monoethanolamine salt, a diethanolamine salt, or a triethanolamine salt
  • ingredients may be synthetic products or commercially available products.
  • examples include ARISTOFLEX AVC (manufactured by Clariant), which corresponds to a vinylpyrrolidone/2-acrylamido-2-methylpropanesulfonic acid (salt) copolymer, SIMULGEL EG (manufactured by SEPIC) and SIMULGEL EPG (manufactured by SEPIC), which each correspond to a sodium acrylate/2-acrylamido-2-methylpropanesulfonic acid (salt) copolymer, SIMULGEL 600 (manufactured by SEPIC) , which corresponds to an acrylamide/2-acrylamido-2-methylpropanesulfonic acid sodium salt copolymer, SEPIGEL 305 (manufactured by SEPIC) and SEPIGEL 501 (manufactured by SEPIC), which each correspond to an acrylamide/2-acrylamido-2-methylpropanesulfonic acid (salt)
  • the content of the ingredient (B) in the skin cosmetic composition of the invention is preferably from 0.1 to 2.0% by mass, more preferably from 0.3 to 1.5% by mass, based on the total amount of the cosmetic composition. If the content is less than 0.1% by mass, a phenomenon such separation, oil floating, demulsification, or aggregation can be more likely to occur, which is not preferred in view of stability. On the other hand, the ingredient (B) added at a content of more than 2.0% by mass will no longer increase the effects of the invention and may contrarily produce a sticky feeling.
  • the ingredient (C) used in the invention may be any ester oil with an IOB value of 0.2 to 0.6.
  • the content of the ingredient (C) in the skin cosmetic composition of the invention is preferably from 1.0 to 15.0% by mass, more preferably from 3.0 to 12.0% by mass, based on the total amount of the cosmetic composition. If the content is less than 1.0% by mass, an advantageous effect of the invention, specifically, suppression of stickiness and production of a penetrating feeling may be insufficient.
  • the ingredient (D) used in the invention may be glycerin commonly used in cosmetics, which may be a synthetic product or a commercially-available product.
  • glycerin which is known to be highly effective in improving the skin but to be sticky, may be used at a content of as relatively high as 5.0 to 15.0% by mass based on the total amount of the cosmetic composition, so that the effect of improving the skin can be reliably obtained.
  • the ingredients (A), (B), and (C) are mixed with it, so that a non-sticky cosmetic composition can be obtained.
  • the oil-in-water type emulsion skin cosmetic composition of the invention may be produced by adding a water-phase component to an oil-phase component and stirring and mixing them by a conventional method with a homogenizer or the like.
  • the water-phase component may contain various water-soluble ingredients in water or in an aqueous phase composed mainly of water.
  • the content of the water-phase component is preferably from 50.0 to 80.0% by mass based on the total amount of the oil-in-water emulsion skin cosmetic composition. If the water-phase component is less than 50.0% by mass, heavy feeling or stickiness may occur. On the other hand, if it is more than 80.0% by mass, the cosmetic composition will be light but not moist, so that a high skin improving effect, an advantageous effect of the invention, can be sometimes hard to obtain.
  • ingredients that can be usually added to emulsion cosmetics may be appropriately added to the oil-in-water type emulsion cosmetic composition of the invention as long as the effects of the invention are not impaired.
  • examples of such other ingredients include, but are not limited to, ultraviolet absorbers, ultraviolet scattering agents, waxes, hydrocarbon oils, fatty acid esters, silicone oils, polyhydric alcohols, water-soluble polymers, higher alcohols, higher fatty acids, and active agents.
  • ultraviolet absorbers examples include p-aminobenzoic acid, octyl-p-methoxycinnamate (2-ethylhexyl-p-methoxycinnamate), glyceryl mono-2-ethylhexanoyl-di-p-methoxycinnamate, methyl bis(trimethylsiloxane)silylisopentyl trimethoxycinnamate, and other cinnamic acid derivative ultraviolet absorbers, 2,2'-hydroxy-5-methylphenylbenzotriazole, 2-(2'-hydroxy-5'-t-octylphenyl)benzotriazole, 2-(2'-hydroxy-5'-methylphenyl benzotriazole, 4-methoxy-4'-t-butyldibenzoylmethane, 5-(3,3-dimethyl-2-norbornylidene)-3-pentan-2-one, bis-ethylhexyloxyphenol-meth
  • ultraviolet scattering agents include fine particles with an average particle size of 10 to 100 nm, such as fine particles of titanium oxide, fine particles of zinc oxide, fine particles of iron oxide, and fine particles of cerium oxide.
  • Ultraviolet scattering agents hydrophobized by a silicone treatment with methyl hydrogen polysiloxane or a silane coupling agent, by a metal soap treatment, by a fluorine treatment with a perfluoroalkylphosphoric acid diethanolamine salt or perfluoroalkylsilane, by a dextrin fatty acid ester treatment, or by other methods may also be added as needed depending on the dosage form.
  • waxes examples include beeswax, candelilla wax, carnauba wax, lanolin, liquid lanolin, and jojoba wax.
  • hydrocarbon oils include liquid paraffin, ozocerite, squalane, pristane, paraffin, ceresin, squalene, petrolatum, microcrystalline wax, polyethylene wax, and Fischer-Tropsch wax.
  • fatty acid esters include cetyl palmitate, cholesteryl stearate, and beeswax fatty acid 2-octyldodecyl ester.
  • silicone oils include chain polysiloxanes (e.g., dimethylpolysiloxane, methylphenylpolysiloxane, and diphenylpolysiloxane); cyclic polysiloxanes (e.g., decamethylcyclopentasiloxane and dodecamethylcyclohexasiloxane), silicone resins forming a three-dimensional network structure, silicone rubbers with an average molecular weight of 200,000 or more, and various modified polysiloxanes (such as amino-modified polysiloxanes, polyether-modified polysiloxanes, alkyl-modified polysiloxanes, and fluorine-modified polysiloxanes).
  • chain polysiloxanes e.g., dimethylpolysiloxane, methylphenylpolysiloxane, and diphenylpolysiloxane
  • cyclic polysiloxanes e.g., de
  • polyhydric alcohols examples include polyethylene glycol, glycerin, diglycerin, 1,3-butylene glycol, erythritol, sorbitol, xylitol, maltitol, 1,2-pentanediol, and hexylene glycol.
  • water-soluble polymers examples include carrageenan, pectin, mannan, curdlan, chondroitin sulfate, starch, glycogen, gum arabic, sodium hyaluronate, tragacanth gum, xanthan gum, mucoitin sulfuric acid, hydroxyethyl guar gum, carboxymethyl guar gum, guar gum, dextran, keratosulfate, locust bean gum, succinoglucan, chitin, chitosan, carboxymethyl chitin, and agar.
  • higher alcohols include hexyl alcohol, octyl alcohol, cetyl alcohol, stearyl alcohol, ceryl alcohol, behenyl alcohol, triacontyl alcohol, cerakyl alcohol, and batyl alcohol.
  • higher fatty acids include lauric acid, myristic acid, palmitic acid, stearic acid, and behenic acid.
  • L-ascorbic acid derivatives include L-ascorbic acid monoalkyl esters such as L-ascorbic acid monostearate, L-ascorbic acid monopalmitate, and L-ascorbic acid monooleate; L-ascorbic acid monoesters such as L-ascorbic acid monophosphate and L-ascorbic acid-2-sulfate; L-ascorbic acid dialkyl esters such as L-ascorbic acid distearate, L-ascorbic acid dipalmitate, and L-ascorbic acid dioleate; L-ascorbic acid trialkyl esters such as L-ascorbic acid tristearate, L-ascorbic acid tripalmitate, and L
  • tranexamic acid derivatives include tranexamic acid dimers (e.g., trans-4-(trans-aminomethylcyclohexanecarbonyl)aminomethylcy clohexanecarboxylic acid hydrochloride), tranexamic acid hydroquinone esters (e.g., 4-(trans-aminomethylcyclohexanecarboxylic acid 4'-hydroxyphenyl ester), tranexamic acid gentisic acid esters (e.g., 2-(trans-4-aminomethylcyclohexylcarbonyloxy)-5-hydroxybenzo ic acid), and tranexamic acid amides (e.g., trans-4-aminomethylcyclohexanecarboxylic acid methylamide, trans-4-(p-methoxybenzoyl)aminomethylcyclohexanecarboxylic acid, and trans-4-guanidinomethylcyclohexanecarboxylic acid).
  • Alkoxysalicylic acid is a salicylic acid derivative in which the hydrogen atom at 3, 4, or 5 position of salicylic acid is replaced by an alkoxy group.
  • the alkoxy group as a substituent is preferably any one of methoxy, ethoxy, propoxy, isopropoxy, butoxy, and isobutoxy groups, more preferably a methoxy group or an ethoxy group.
  • alkoxysalicylic acid and a derivative thereof are each preferably used in the form of a salt.
  • the salts of drugs include, but are not limited to, alkali metal or alkaline-earth metal salts such as sodium salts, potassium salts, and calcium salts, and other salts such as ammonium salts and amino acid salts.
  • ingredients that may be added also include vitamin A, vitamin A derivatives such as vitamin A palmitate and vitamin A acetate, vitamin B6 hydrochloride, vitamin B 6 tripalmitate, vitamin B 6 dioctanoate, vitamin B 2 and derivatives thereof, vitamin B 12 , vitamin B 15 and derivatives thereof, and other vitamin B materials, ⁇ -tocopherol, ⁇ -tocopherol, vitamin E acetate, and other vitamin E materials, vitamin D materials, vitamin H, pantothenic acid, pantethine, and other vitamins; ⁇ -oryzanol, allantoin, glycyrrhizinic acid (salt), glycyrrhetinic acid, stearyl glycyrrhetinate, hinokitiol, bisabolol, eukalypton, thymol, inositol, saikosaponin, carrot saponin, sponge gourd saponin, mukurossi peel saponin, and
  • ingredients also include lower alcohols such as ethanol; antioxidants such as butylhydroxytoluene, ⁇ -tocopherol, and phytin; preservatives such as benzoic acid, salicylic acid, sorbic acid, alkyl p-oxybenzoate, phenoxyethanol, hexachlorophene, ands-polylysine; and organic or inorganic acids such as citric acid, lactic acid, and hexametaphosphoric acid, and salts thereof.
  • lower alcohols such as ethanol
  • antioxidants such as butylhydroxytoluene, ⁇ -tocopherol, and phytin
  • preservatives such as benzoic acid, salicylic acid, sorbic acid, alkyl p-oxybenzoate, phenoxyethanol, hexachlorophene, ands-polylysine
  • organic or inorganic acids such as citric acid, lactic acid, and hexametaphosphoric acid, and salts thereof
  • oils-in-water type emulsion skin cosmetic composition of the invention include, but are not limited to, skin milk, skin cream, hair cream, liquid foundation, eye liner, mascara, eye shadow, and any other milky or creamy products.
  • a panel of female experts carried out an actual use test to evaluate speadability on skin and made evaluations according to the criteria below.
  • a panel of female experts carried out an actual use test to evaluate stickiness and made evaluations according to the criteria below.
  • a panel of female experts carried out an actual use test to evaluate lightness and made evaluations according to the criteria below.
  • a panel of female experts carried out an actual use test to evaluate skin resilience and made evaluations according to the criteria below.
  • a panel of female experts carried out an actual use test to evaluate the effect of moisturizing the skin and made evaluations according to the criteria below.
  • oil-in-water type emulsion skin cosmetic creams were prepared by a conventional method.
  • the resulting compositions were evaluated for stability, texture, and skin improving effect according to the methods and criteria described above.
  • "vinylpyrrolidone/sodium 2-acrylamido-methylpropanesulfonate copolymer” used as the “ingredient (B)” was "ARISTOFLEX AVC” (manufactured by CLARIANT).
  • Example 1 Ingredients Example 1 2 3 4 5 6 7 (1) Ion-exchanged water Balance Balance Balance Balance Balance Balance Balance Balance Balance Balance (2) D-alanine [ingredient (A)] 0.1 3.0 5.0 0.1 3.0 3.0 3.0 (3) Glycerin [ingredient (D)] 5.0 10.0 15.0 10.0 5.0 10.0 10.0 (4) 1,3-butylene glycol 3.0 3.0 3.0 3.0 3.0 3.0 (5) Vinylpyrrolidone/sodium 2-acrylamido-methylpropanesulfonate copolymer [ingredient (B)] 0.1 1.0 2.0 1.0 1.0 0.1 1.0 (5') Carboxyvinyl polymer - - - - - - - (6) Self-emulsitying glyceryl monostearate 3.0 3.0 3.0 3.0 3.0 3.0 (7) PEG-100 stearate 2.0 2.0 2.0 2.0 2.0 2.0 2.0 2.0 2.0 2.0 2.0 2.0 2.0 (8) Stearic acid 0.1 0.1 0.1 0.1 0.1 0.1
  • Tables 1 and 2 show that Examples 1 to 7 according to the invention are excellent in stability, texture, and skin improving effect. In contrast, not all of stability, texture, and skin improving effect are satisfactory with respect to Comparative Examples 1 to 6, which do not satisfy the requirements of the invention. Specifically, Comparative Examples 1 to 3 and 6 lack any of the ingredients (A) , (B) , (C) , and (D) . Comparative Example 1 not containing the ingredient (A) is sticky and lacks a skin moisturizing effect. Comparative Example 2 not containing the ingredient (B) particularly has a problem with stability. Comparative Example 3 not containing the ingredient (C) is significantly inferior in texture such as spreadability on skin, stickiness, or lightness. Comparative Example 6 not containing the ingredient (D) does not produce a skin improving effect such as a skin moisturizing effect.
  • Comparative Example 4 containing another thickener (carboxyvinyl polymer) instead of the ingredient (B) is insufficient in texture with respect to stickiness, lightness, etc. and insufficient in skin improving effect.
  • Comparative Example 5 containing squalane with an IOB of 0 instead of the ingredient (C) is sticky and lacks spreadability on skin and lightness, although it makes the skin resilient and moisturized.
  • ingredients (1) to (8) were uniformly mixed and dissolved at 70°C (oil phase) .
  • ingredients (9) to (18) were uniformly mixed and dissolved at 70°C (aqueous phase) .
  • the oil phase was gradually added to the aqueous phase kept at 70°C, the mixture was emulsified with a homomixer. After the emulsification was completed, the emulsion was rapidly cooled to 40°C or less to give the desired anti-aging cream.
  • the resulting cream was evaluated in the same manner as described above for Examples 1 to 7. As a result, the cream had good texture (the evaluation was ⁇ with respect to all of skin spreadability, stickiness, and lightness) , a moisturizing effect, light spreadability, and a moist feeling with lightness when applied to the skin, and also had good stability (the stability was evaluated "O").
  • ingredients (1) to (9) were uniformly mixed and dissolved at 70°C (oil phase).
  • ingredients (10) to (16) were uniformly mixed and dissolved at 70°C (aqueous phase) . While the oil phase was gradually added to the aqueous phase kept at 70°C, the mixture was emulsified with a homomixer. After the emulsification was completed, the emulsion was rapidly cooled to 40°C or less to give the desired O/W emulsion type sunscreen.
  • the resulting sunscreen was evaluated in the same manner as Examples 1 to 7. As a result, the sunscreen had good texture (the evaluation was ⁇ with respect to all of skin spreadability, stickiness, and lightness), a moisturizing effect, light spreadability, and a moist feeling with lightness when applied to the skin, and also had good stability (the stability was evaluated "O") .
  • ingredients (1) to (7) were uniformly mixed and dissolved at 70°C (oil phase).
  • ingredients (8) to (19) were uniformly mixed and dissolved at 70°C (aqueous phase). While the oil phase was gradually added to the aqueous phase kept at 70°C, the mixture was emulsified with a homomixer. After the emulsification was completed, the emulsion was rapidly cooled to 40°C or less to give the desired whitening cream.
  • the resulting whitening cream was evaluated in the same manner as Examples 1 to 7.
  • the cream had good texture (the evaluation was ⁇ with respect to all of skin spreadability, stickiness, and lightness), a moisturizing effect, light spreadability, and a moist feeling with lightness when applied to the skin, and also had good stability (the stability was evaluated "O").
  • ingredients (1) to (8) were uniformly mixed and dissolved at 70°C (oil phase).
  • ingredients (9) to (20) were uniformly mixed and dissolved at 70°C (aqueous phase). While the oil phase was gradually added to the aqueous phase kept at 70°C, the mixture was emulsified with a homomixer. After the emulsification was completed, the emulsion was rapidly cooled to 40°C or less to give the desired whitening cream.
  • the resulting whitening cream was evaluated in the same manner as Examples 1 to 7.
  • the cream had good texture (the evaluation was ⁇ with respect to all of skin spreadability, stickiness, and lightness), a moisturizing effect, light spreadability, and a moist feeling with lightness when applied to the skin, and also had good stability (the stability was evaluated "O").

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Animal Behavior & Ethology (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Emergency Medicine (AREA)
  • Dermatology (AREA)
  • Chemical & Material Sciences (AREA)
  • Dispersion Chemistry (AREA)
  • Cosmetics (AREA)

Abstract

Disclosed is an oil-in-water type emulsion skin cosmetic which can be spread on skin easily, is not sticky, has an excellent feeling as an active ingredient penetrates into skin, can enrich skin, can moisturize skin, and can exhibit a high skin improvement effect due to glycerin contained therein, when prepared in the form of a formulation containing glycerin at a high concentration or a formulation containing a combination of glycerin and an acrylamide-type thickening agent. The skin cosmetic is characterized by comprising (A) a D-amino acid or a derivative or salt thereof, (B) a homopolymer, a copolymer or a crosspolymer containing at least one component selected from 2-acrylamide-2-methylpropanesulfonic acid, acrylic acid and derivatives thereof as a constituent unit, (C) an ester oil with an IOB value of 0.2 to 0.6, and (D) glycerin.

Description

    TECHNICAL FIELD
  • The invention relates to an oil-in-water type emulsion skin cosmetic composition having good texture and stability. More specifically, the invention relates to an oil-in-water type emulsion skin cosmetic composition having light spreadability on skin, no stickiness, lightness, a good feeling as an active ingredient effectively penetrates into the skin (good penetrating feeling), and high stability over time.
  • BACKGROUND ART
  • Glycerin is known as a cosmetic ingredient having a high moisturizing effect and a high skin improving effect such as a high skin roughness reducing effect. To produce such a high skin improving effect significantly, glycerin is often added at a content of 5.0% by mass or more. Particularly, skin cosmetics with high glycerin content can produce high skin improving effect but may have the disadvantage in use that as the content increases, dewy feeling or feeling as an active ingredient penetrates into the skin disappears, and stickiness appears.
  • In recent years, there have been attempts, such as the addition of fatty acid glycerin ester, the addition of specific water-soluble solid silicone, and the addition of organosiloxane elastomer spherical particles, to reduce stickiness caused by the addition of glycerin and to obtain a light feeling (see Patent Documents 1 to 3).
  • However, these conventional techniques tend to reduce the skin improving effect of glycerin in conflict with a certain stickiness reducing effect produced by the addition of the above additive.
  • On the other hand, acrylamide thickeners, which are used as cosmetic thickeners, provide good texture such as good compatibility to the skin or good spreadability (see for example Patent Documents 4 and 5). Such acrylamide thickeners are useful as an alternative to carboxyvinyl polymer, xanthan gum, or hydroxyethyl cellulose, which is traditionally used as a cosmetic thickener in many cases. However, when glycerin is added at a high concentration to provide a skin improving effect, a problem also occurs in which good texture of acrylamide thickeners is lost and it becomes impossible to reduce the glycerin-induced stickiness.
  • PRIOR ART PUBLICATIONS PATENT DOCUMENTS
    • Patent Document 1: JP-A Hei 11-246329
    • Patent Document 2: JP-A 2000-191428
    • Patent Document 3: JP-A 2002-356416
    • Patent Document 4: JP-A Hei 10-67685
    • Patent Document 5: JP-A 2001-114641
    SUMMARY OF INVENTION PROBLEMS TO BE SOLVED BY THE INVENTION
  • It is therefore an object of the invention to solve the conventional problems and to provide an oil-in-water type emulsion skin cosmetic composition that has light spreadability on skin, no stickiness, and a good penetrating feeling as an active ingredient effectively penetrates into the skin, provides moisture, and is moist even in a system with a high glycerin content or in a system used in combination with an acrylamide thickener, and also allows glycerin to produce a high skin improving effect.
  • MEANS FOR SOLVING THE PROBLEMS
  • As a result of earnest studies to solve the problems, the present inventors have accomplished the invention based on the finding that even in a system with a high glycerin content, an oil-in-water type emulsion skin cosmetic composition containing (A) a D-amino acid or a derivative or salt thereof, (B) a homopolymer, a copolymer, or a crosspolymer including, as a constituent unit, one or more selected from 2-acrylamido-2-methylpropanesulfonic acid, acrylic acid, and derivatives thereof, (C) an ester oil with an IOB value of 0.2 to 0.6, and (D) glycerin is compatible to the skin and not sticky during use, and can reliably produce a skin improving effect.
  • EFFECTS OF THE INVENTION
  • According to the invention, there is provided an oil-in-water type emulsion skin cosmetic composition that has light spreadability on skin, no stickiness, and a good penetrating feeling when an active ingredient penetrates the skin, provides moisture, and is moist even in a system with a high glycerin content, and also allows glycerin to produce a high skin improving effect.
  • MODES FOR CARRYING OUT THE INVENTION
  • Hereinafter, the invention is described in detail.
    The skin cosmetic composition of the invention essentially contains a D-amino acid or a derivative or salt thereof (ingredient (A), hereinafter also abbreviated as "D-amino acid maternal"). As used herein, the term "D-amino acid or a derivative or salt thereof (D-amino acid material)" means a D-amino acid, a derivative thereof, a salt thereof, or a mixture thereof.
  • It is well known that amino acids can exist in L-form or D-form which are optical isomers and natural proteins are composed of L-amino acids bonded together by peptide bonds. It has been considered that except for some cases such as bacterial cell walls, only L-amino acids exist in mammals including human and only L-amino acids are used in living bodies. Conventionally, therefore, academic or industrial focus and research have been dominantly on L-amino acids.
    Exceptional cases where D-amino acids are used include (1) cases where D-amino acids are used as raw materials for antibiotics to be produced by bacteria and (2) cases where food additives contain a mixture of L- and D-amino acids in order to avoid the cost required to isolate the L-amino acid from the mixture (racemic mixture) containing equal amounts of the Land D-amino acids synthesized chemically.
  • Recently, it has been found that even in the human body, D-aspartic acid (D-Asp), which does not occur naturally, increases with age in the ocular lens, brain, or skin, and the relationship between it and the development of cataract or Alzheimer's disease has begun to be discussed (Tadatoshi Kinouchi et al. "proteins, Nucleic Acids, and Enzymes" (in Japanese) Vol. 50, No. 5 (2005), 453-560). Also in the skin, accumulation of D-Asp has been found to be caused by aging or ultraviolet irradiation, and it has been proposed that D-Asp be used as a molecular marker for detecting skin damage caused by aging or ultraviolet rays (Noriko Fujii, Annual Report of Cosmetology (in Japanese) , No. 13 (2005 ) . However, no examples are known in which D-amino acids are positively used as biologically active materials.
    Under the above circumstances, the invention is characterized in that a D-amino acid, which has not been conventionally added to cosmetics, especially skin cosmetics, is added as an essential ingredient.
  • The D-amino acid material (ingredient (A)) used in the invention may be of any type as long as it is in the D-form. Preferably, the D-amino acid material itself can be effective in improving the skin. Examples include D-aspartic acid, which can have an antioxidant effect and a collagen production promoting effect, D-alanine, which can have a laminin 332 production promoting effect and a collagen production promoting effect, D-glutamic acid, which can have a barrier recovery function, a wrinkle formation reducing effect, and a skin roughness reducing effect, D-serine, which can have an ultraviolet damage reducing effect, D-hydroxyproline, which can have a laminin 332 production promoting effect, D-cysteine, which can have an ultraviolet damage reducing effect, D-methionine and D-proline, which can have an ultraviolet damage reducing effect, and D-hydroxyproline, which can have a melanin production inhibiting effect.
  • The D-amino acid material used in the invention may be a synthetic product or a commercially available product.
    For example, a known method for producing a D-amino acid includes allowing bacterial D-aminoacylase to act on an acylated amino acid to obtain a D-amino acid (see JP-A Hei 11-113592 ).
    The content of the D-amino acid material in the skin cosmetic composition of the invention is preferably from 0.1 to 5.0% by mass based on the total amount of the cosmetic composition.
  • Next, a detailed description is given of a homopolymer, a copolymer, or a crosspolymer including, as a constituent unit, one or more selected from 2-acrylamido-2-methylpropanesulfonic acid (hereinafter also abbreviated as "AMPS"), acrylic acid, and derivatives thereof, which is used as the ingredient (B) in the invention.
  • Examples of the ingredient (B) used in the invention include a vinylpyrrolidone/2-acrylamido-2-methylpropanesulfonic acid (salt) copolymer, a dimethylacrylamide/2-acrylamido-2-methylpropanesulfonic acid (salt) copolymer, an acrylamide/2-acrylamido-2-methylpropanesulfonic acid copolymer, a methylenebisacrylamide-crosslinked dimethylacrylamide/2-acrylamido-2-methylpropanesulfonic acid crosspolymer, a mixture of polyacrylamide and poly (sodium acrylate), a sodium acrylate/2-acrylamido-2-methylpropanesulfonic acid copolymer, a hydroxyethyl acrylate/2-acrylamido-2-methylpropanesulfonic acid (salt) copolymer, poly(ammonium acrylate), a polyacrylamide/ammonium acrylate copolymer, and an acrylamide/sodium acrylate copolymer. It will be understood that these are non-limiting examples.
    In the above polymers, preferred examples of the salt include an alkali metal salt (such as a calcium salt or a magnesium salt), an ammonium salt, and an organic amine salt (such as a monoethanolamine salt, a diethanolamine salt, or a triethanolamine salt). One or more of these (B) ingredients may be used.
  • These (B) ingredients may be synthetic products or commercially available products. Examples include ARISTOFLEX AVC (manufactured by Clariant), which corresponds to a vinylpyrrolidone/2-acrylamido-2-methylpropanesulfonic acid (salt) copolymer, SIMULGEL EG (manufactured by SEPIC) and SIMULGEL EPG (manufactured by SEPIC), which each correspond to a sodium acrylate/2-acrylamido-2-methylpropanesulfonic acid (salt) copolymer, SIMULGEL 600 (manufactured by SEPIC) , which corresponds to an acrylamide/2-acrylamido-2-methylpropanesulfonic acid sodium salt copolymer, SEPIGEL 305 (manufactured by SEPIC) and SEPIGEL 501 (manufactured by SEPIC), which each correspond to an acrylamide/2-acrylamido-2-methylpropanesulfonic acid (salt) copolymer, Hostacerin AMPS (manufactured by Clariant) and SIMULGEL 800 (manufactured by SEPIC), which each correspond to a homopolymer of 2-acrylamido-2-methylpropanesulfonic acid sodium salt, and SU-POLYMER G-1 (manufactured by TOHO Chemical Industry Co., Ltd.), which corresponds to a dimethylacrylamide/2-acrylamido-2-methylpropanesulfonic acid copolymer.
  • The content of the ingredient (B) in the skin cosmetic composition of the invention is preferably from 0.1 to 2.0% by mass, more preferably from 0.3 to 1.5% by mass, based on the total amount of the cosmetic composition. If the content is less than 0.1% by mass, a phenomenon such separation, oil floating, demulsification, or aggregation can be more likely to occur, which is not preferred in view of stability. On the other hand, the ingredient (B) added at a content of more than 2.0% by mass will no longer increase the effects of the invention and may contrarily produce a sticky feeling.
  • Next, a detailed description is given of an ester oil with an IOB value of 0.2 to 0.6, the ingredient (C), used in the invention.
    The ingredient (C) used in the invention may be any ester oil with an IOB value of 0.2 to 0.6. Examples include tripropylene glycol dineopentanoate (IOB=0.52), isodecyl benzoate (IOB=0.23), propylene glycol dicaprylate (IOB=0.32), isononyl isononanoate (IOB=0.2), cetyl 2-ethylhexanoate (IOB=0.52), glyceryl tri-2-ethylhexanoate (IOB=0.36), isodecyl neopentanoate (IOB=0.22), 2-ethylhexyl 2-ethylhexanoate (IOB=0.2), pentaerythritol tetra-2-ethylhexanoate (IOB=0.35), di-2-ethylhexyl succinate (IOB=0.32), and 2-ethylhexyl isononanoate (IOB=0.2).
  • One or more of these ester oils may be used.
    Particularly in view of texture, the content of the ingredient (C) in the skin cosmetic composition of the invention is preferably from 1.0 to 15.0% by mass, more preferably from 3.0 to 12.0% by mass, based on the total amount of the cosmetic composition. If the content is less than 1.0% by mass, an advantageous effect of the invention, specifically, suppression of stickiness and production of a penetrating feeling may be insufficient.
  • Next, a description is given of glycerin, the ingredient (D), used in the invention.
    The ingredient (D) used in the invention may be glycerin commonly used in cosmetics, which may be a synthetic product or a commercially-available product.
    In the invention, glycerin (the ingredient (D)), which is known to be highly effective in improving the skin but to be sticky, may be used at a content of as relatively high as 5.0 to 15.0% by mass based on the total amount of the cosmetic composition, so that the effect of improving the skin can be reliably obtained. On the other hand, the ingredients (A), (B), and (C) are mixed with it, so that a non-sticky cosmetic composition can be obtained.
  • The oil-in-water type emulsion skin cosmetic composition of the invention may be produced by adding a water-phase component to an oil-phase component and stirring and mixing them by a conventional method with a homogenizer or the like. The water-phase component may contain various water-soluble ingredients in water or in an aqueous phase composed mainly of water. The content of the water-phase component is preferably from 50.0 to 80.0% by mass based on the total amount of the oil-in-water emulsion skin cosmetic composition. If the water-phase component is less than 50.0% by mass, heavy feeling or stickiness may occur. On the other hand, if it is more than 80.0% by mass, the cosmetic composition will be light but not moist, so that a high skin improving effect, an advantageous effect of the invention, can be sometimes hard to obtain.
  • Besides the above essential ingredients, other ingredients that can be usually added to emulsion cosmetics may be appropriately added to the oil-in-water type emulsion cosmetic composition of the invention as long as the effects of the invention are not impaired.
    Examples of such other ingredients include, but are not limited to, ultraviolet absorbers, ultraviolet scattering agents, waxes, hydrocarbon oils, fatty acid esters, silicone oils, polyhydric alcohols, water-soluble polymers, higher alcohols, higher fatty acids, and active agents.
  • Examples of ultraviolet absorbers include p-aminobenzoic acid, octyl-p-methoxycinnamate (2-ethylhexyl-p-methoxycinnamate), glyceryl mono-2-ethylhexanoyl-di-p-methoxycinnamate, methyl bis(trimethylsiloxane)silylisopentyl trimethoxycinnamate, and other cinnamic acid derivative ultraviolet absorbers, 2,2'-hydroxy-5-methylphenylbenzotriazole, 2-(2'-hydroxy-5'-t-octylphenyl)benzotriazole, 2-(2'-hydroxy-5'-methylphenyl benzotriazole, 4-methoxy-4'-t-butyldibenzoylmethane, 5-(3,3-dimethyl-2-norbornylidene)-3-pentan-2-one, bis-ethylhexyloxyphenol-methoxyphenyl-triazine, 2,4,6-tris[4-(2-ethylhexyloxycarbonyl)anilino]1,3,5-triazin e, dimorpholinopyridazinone, and 2-ethylhexyl-2-cyano-3,3-diphenylacrylate.
  • Examples of ultraviolet scattering agents include fine particles with an average particle size of 10 to 100 nm, such as fine particles of titanium oxide, fine particles of zinc oxide, fine particles of iron oxide, and fine particles of cerium oxide.
    Ultraviolet scattering agents hydrophobized by a silicone treatment with methyl hydrogen polysiloxane or a silane coupling agent, by a metal soap treatment, by a fluorine treatment with a perfluoroalkylphosphoric acid diethanolamine salt or perfluoroalkylsilane, by a dextrin fatty acid ester treatment, or by other methods may also be added as needed depending on the dosage form.
  • Examples of waxes include beeswax, candelilla wax, carnauba wax, lanolin, liquid lanolin, and jojoba wax.
    Examples of hydrocarbon oils include liquid paraffin, ozocerite, squalane, pristane, paraffin, ceresin, squalene, petrolatum, microcrystalline wax, polyethylene wax, and Fischer-Tropsch wax.
    Examples of fatty acid esters include cetyl palmitate, cholesteryl stearate, and beeswax fatty acid 2-octyldodecyl ester.
  • Examples of silicone oils include chain polysiloxanes (e.g., dimethylpolysiloxane, methylphenylpolysiloxane, and diphenylpolysiloxane); cyclic polysiloxanes (e.g., decamethylcyclopentasiloxane and dodecamethylcyclohexasiloxane), silicone resins forming a three-dimensional network structure, silicone rubbers with an average molecular weight of 200,000 or more, and various modified polysiloxanes (such as amino-modified polysiloxanes, polyether-modified polysiloxanes, alkyl-modified polysiloxanes, and fluorine-modified polysiloxanes).
  • Examples of polyhydric alcohols include polyethylene glycol, glycerin, diglycerin, 1,3-butylene glycol, erythritol, sorbitol, xylitol, maltitol, 1,2-pentanediol, and hexylene glycol.
    Examples of water-soluble polymers include carrageenan, pectin, mannan, curdlan, chondroitin sulfate, starch, glycogen, gum arabic, sodium hyaluronate, tragacanth gum, xanthan gum, mucoitin sulfuric acid, hydroxyethyl guar gum, carboxymethyl guar gum, guar gum, dextran, keratosulfate, locust bean gum, succinoglucan, chitin, chitosan, carboxymethyl chitin, and agar.
  • Examples of higher alcohols include hexyl alcohol, octyl alcohol, cetyl alcohol, stearyl alcohol, ceryl alcohol, behenyl alcohol, triacontyl alcohol, cerakyl alcohol, and batyl alcohol.
    Examples of higher fatty acids include lauric acid, myristic acid, palmitic acid, stearic acid, and behenic acid.
  • Example of active agents include salts of L-ascorbic acid and derivatives thereof, salts of tranexamic acid and derivatives thereof, salts of alkoxysalicylic acid and derivatives thereof, and salts of glutathione and derivatives thereof. More specifically, L-ascorbic acid derivatives include L-ascorbic acid monoalkyl esters such as L-ascorbic acid monostearate, L-ascorbic acid monopalmitate, and L-ascorbic acid monooleate; L-ascorbic acid monoesters such as L-ascorbic acid monophosphate and L-ascorbic acid-2-sulfate; L-ascorbic acid dialkyl esters such as L-ascorbic acid distearate, L-ascorbic acid dipalmitate, and L-ascorbic acid dioleate; L-ascorbic acid trialkyl esters such as L-ascorbic acid tristearate, L-ascorbic acid tripalmitate, and L-ascorbic acid trioleate; L-ascorbic acid triesters such as L-ascorbic acid triphosphate; and L-ascorbic acid glucosides such as L-ascorbic acid 2-glucoside. In the invention, L-ascorbic acid, L-ascorbic acid phosphate, L-ascorbic acid-2-sulfate, and L-ascorbic acid 2-glucoside are each preferably used in the form of a salt.
  • Examples of tranexamic acid derivatives include tranexamic acid dimers (e.g., trans-4-(trans-aminomethylcyclohexanecarbonyl)aminomethylcy clohexanecarboxylic acid hydrochloride), tranexamic acid hydroquinone esters (e.g., 4-(trans-aminomethylcyclohexanecarboxylic acid 4'-hydroxyphenyl ester), tranexamic acid gentisic acid esters (e.g., 2-(trans-4-aminomethylcyclohexylcarbonyloxy)-5-hydroxybenzo ic acid), and tranexamic acid amides (e.g., trans-4-aminomethylcyclohexanecarboxylic acid methylamide, trans-4-(p-methoxybenzoyl)aminomethylcyclohexanecarboxylic acid, and trans-4-guanidinomethylcyclohexanecarboxylic acid). In the invention, tranexamic acid or a tranexamic acid derivative is preferably used in the form of a salt.
  • Alkoxysalicylic acid is a salicylic acid derivative in which the hydrogen atom at 3, 4, or 5 position of salicylic acid is replaced by an alkoxy group. The alkoxy group as a substituent is preferably any one of methoxy, ethoxy, propoxy, isopropoxy, butoxy, and isobutoxy groups, more preferably a methoxy group or an ethoxy group. Examples of such a compound include 3-methoxysalicylic acid, 3-ethoxysalicylic acid, 4-methoxysalicylic acid, 4-ethoxysalicylic acid, 4-propoxysalicylic acid, 4-isopropoxysalicylic acid, 4-butoxysalicylic acid, 5-methoxysalicylic acid, 5-ethoxysalicylic acid, and 5-propoxysalicylic acid. In the invention, alkoxysalicylic acid and a derivative thereof (such as an ester) are each preferably used in the form of a salt.
    Examples of the salts of drugs include, but are not limited to, alkali metal or alkaline-earth metal salts such as sodium salts, potassium salts, and calcium salts, and other salts such as ammonium salts and amino acid salts.
  • Other ingredients that may be added also include vitamin A, vitamin A derivatives such as vitamin A palmitate and vitamin A acetate, vitamin B6 hydrochloride, vitamin B6 tripalmitate, vitamin B6 dioctanoate, vitamin B2 and derivatives thereof, vitamin B12, vitamin B15 and derivatives thereof, and other vitamin B materials, α-tocopherol, β-tocopherol, vitamin E acetate, and other vitamin E materials, vitamin D materials, vitamin H, pantothenic acid, pantethine, and other vitamins; γ-oryzanol, allantoin, glycyrrhizinic acid (salt), glycyrrhetinic acid, stearyl glycyrrhetinate, hinokitiol, bisabolol, eukalypton, thymol, inositol, saikosaponin, carrot saponin, sponge gourd saponin, mukurossi peel saponin, and other saponins, pantothenyl ethyl ether, arbutin, cepharanthine, and other various medicines, extracts of plants such as curly dock, sophora, Nuphar, orange, sage, yarrow, mallow, swertia herb, thyme, Japanese angelica root, spruce, white birch, horsetail, sponge gourd, horse chestnut, saxifrage, scutellaria root, arnica, lily, mugwort, peony, aloe, gardenia, and cherry leaf, and β-carotene and other colorants.
  • Other ingredients also include lower alcohols such as ethanol; antioxidants such as butylhydroxytoluene, δ-tocopherol, and phytin; preservatives such as benzoic acid, salicylic acid, sorbic acid, alkyl p-oxybenzoate, phenoxyethanol, hexachlorophene, ands-polylysine; and organic or inorganic acids such as citric acid, lactic acid, and hexametaphosphoric acid, and salts thereof.
  • Examples of the form of the oil-in-water type emulsion skin cosmetic composition of the invention include, but are not limited to, skin milk, skin cream, hair cream, liquid foundation, eye liner, mascara, eye shadow, and any other milky or creamy products.
  • EXAMPLES
  • Hereinafter, the invention is more specifically described with reference to examples, which however are not intended to limit the invention. All material content percentages are by mass unless otherwise specified.
    First, a description is given of the evaluation methods used for the invention.
  • [Stability Test]
  • Samples were allowed to stand at 50°C for one month, and then their appearances were visually observed and evaluated according to the criteria below.
  • (Evaluation Criteria)
    • O: Separation was not observed at all.
    • Δ: Separation was hardly observed.
    • ×: Separation in Liquid-phase (oil-phase or aqueous-phase) occurred.
    [Texture (Spreadability on skin)]
  • A panel of female experts (ten experts) carried out an actual use test to evaluate speadability on skin and made evaluations according to the criteria below.
  • (Evaluation Criteria)
    • ⊙: All ten experts determined that spreading was light and smooth.
    • O: Seven to nine experts determined that spreading was light and smooth.
    • Δ: Three to six experts determined that spreading was light and smooth.
    • ×: Zero to two experts determined that spreading was light and smooth.
    [Texture (stickiness)]
  • A panel of female experts (ten experts) carried out an actual use test to evaluate stickiness and made evaluations according to the criteria below.
  • (Evaluation Criteria)
    • ⊙: All ten experts determined that there was a moist feeing with no stickiness.
    • O: Seven to nine experts determined that there was a moist feeing with no stickiness.
    • Δ: Three to six experts determined that there was a moist feeing with no stickiness.
    • ×: Zero to two experts determined that there was a moist feeing with no stickiness.
    [Texture (Lightness)]
  • A panel of female experts (ten experts) carried out an actual use test to evaluate lightness and made evaluations according to the criteria below.
  • (Evaluation Criteria)
    • ⊙: All ten experts determined that there was lightness.
    • O: Seven to nine experts determined that there was lightness.
    • ΔL: Three to six experts determined that there was lightness.
    • ×: Zero to two experts determined that there was lightness.
    [Skin Improving Effect (Skin Resilience)]
  • A panel of female experts (ten experts) carried out an actual use test to evaluate skin resilience and made evaluations according to the criteria below.
  • (Evaluation Criteria)
    • ⊙: All ten experts determined that the skin became resilient.
    • O: Seven to nine experts determined that the skin became resilient.
    • Δ: Three to six experts determined that the skin became resilient.
    • ×: Zero to two experts determined that the skin became resilient.
    [Skin Improving Effect (Making Skin Moisturized)]
  • A panel of female experts (ten experts) carried out an actual use test to evaluate the effect of moisturizing the skin and made evaluations according to the criteria below.
  • (Evaluation Criteria)
    • ⊙: All ten experts determined that the skin was made moisturized.
    • O: Seven to nine experts determined that the skin was made moisturized.
    • Δ: Three to six experts determined that the skin was made moisturized.
    • ×: Zero to two experts determined that the skin was made moisturized.
    (Examples 1 to 7 and Comparative Examples 1 to 6)
  • According to the formulas shown in Tables 1 and 2 below, oil-in-water type emulsion skin cosmetic creams were prepared by a conventional method. The resulting compositions (samples) were evaluated for stability, texture, and skin improving effect according to the methods and criteria described above.
    In Tables 1 and 2, "vinylpyrrolidone/sodium 2-acrylamido-methylpropanesulfonate copolymer" used as the "ingredient (B)" was "ARISTOFLEX AVC" (manufactured by CLARIANT).
  • [Table 1]
    Ingredients Example
    1 2 3 4 5 6 7
    (1) Ion-exchanged water Balance Balance Balance Balance Balance Balance Balance
    (2) D-alanine [ingredient (A)] 0.1 3.0 5.0 0.1 3.0 3.0 3.0
    (3) Glycerin [ingredient (D)] 5.0 10.0 15.0 10.0 5.0 10.0 10.0
    (4) 1,3-butylene glycol 3.0 3.0 3.0 3.0 3.0 3.0 3.0
    (5) Vinylpyrrolidone/sodium 2-acrylamido-methylpropanesulfonate copolymer [ingredient (B)] 0.1 1.0 2.0 1.0 1.0 0.1 1.0
    (5') Carboxyvinyl polymer - - - - - - -
    (6) Self-emulsitying glyceryl monostearate 3.0 3.0 3.0 3.0 3.0 3.0 3.0
    (7) PEG-100 stearate 2.0 2.0 2.0 2.0 2.0 2.0 2.0
    (8) Stearic acid 0.1 0.1 0.1 0.1 0.1 0.1 0.1
    (9) Palmitic acid 0.3 0.3 0.3 0.3 0.3 0.3 0.3
    (10) Sodium hydroxide Proper amount Proper amount Proper amount Proper amount Proper amount Proper amount Proper amount
    (11) Myristyl myristate 2.0 2.0 2.0 2.0 2.0 2.0 2.0
    (12) Isodecyl neopentanoate [ingredient (C)] 1.0 8.0 15.0 8.0 10.0 1.0 1.0
    (13) Squalane - - - - - - -
    (14) Dimethylsilicone (5 mPa·s) 5.0 5.0 5.0 5.0 5.0 5.0 5.0
    (15) Hydrogenated polyisobutene 5.0 5.0 5.0 5.0 5.0 5.0 5.0
    (16) 2-ethylhexyl-2-cyano-3,3-diphenylacrylate 1.0 1.0 1.0 1.0 1.0 1.0 1.0
    (17) Edetate 0.1 0.1 0.1 0.1 0.1 0.1 0.1
    (18) Phenoxyethanol 0.5 0.5 0.5 0.5 0.5 0.5 0.5
    (19) Perfume 0.1 0.1 0.1 0.1 0.1 0.1 0.1
    Stability
    Texture (Spreadability on skin)
    (stickiness)
    (lightness)
    Skin improving effect (skin resilience)
    (skin moisturizing)
  • [Table 2]
    Ingredients Example
    1 2 3 4 5 6
    (1) Ion-exchanged water Balance Balance Balance Balance Balance Balance
    (2) D-alanine [ingredient (A)] - 3.0 3.0 1.0 3.0 3.0
    (3) Glycerin [ingredient (D)] 5.0 5.0 5.0 5.0 5.0 -
    (4) 1,3-butylene glycol 3.0 3.0 3.0 3.0 3.0 3.0
    (5) Vinylpyrrolidone/sodium 2-acrylamido-methylpropanesulfonate copolymer [ingredient (B)] 1.0 - 1.0 - 1.0 1.0
    (5') Carboxyvinyl polymer - - - 0.2 - -
    (6) Self-emulsifying glyceryl monostearate 3.0 3.0 3.0 3.0 3.0 3.0
    (7) PEG-100 stearate 2.0 2.0 2.0 2.0 2.0 2.0
    (8) Stearic acid 0.1 0.1 0.1 0.1 0.1 0.1
    (9) Palmitic acid 0.3 0.3 0.3 0.3 0.3 0.3
    (10) Sodium hydroxide Proper amount Proper amount Proper amount Proper amount Proper amount Proper amount
    (11) Myristyl myristate 2.0 2.0 2.0 2.0 2.0 2.0
    (12) Isodecyl neopentanoate [ingredient (C)] 8.0 8.0 - 8.0 - 8.0
    (13) Squalane - - - - 8.0 -
    (14) Dimethylsilicone (5 mPa·s) 5.0 5.0 5.0 5.0 5.0 5.0
    (15) Hydrogenated polyisobutene 5.0 5.0 5.0 5.0 5.0 5.0
    (16) 2-ethylhexyl-2-cyano-3,3-diphenylacrylate 1.0 1.0 1.0 1.0 1.0 1.0
    (17) Edetate 0.1 0.1 0.1 0.1 0.1 0.1
    (18) Phenoxyethanol 0.5 0.5 0.5 0.5 0.5 0.5
    (19) Perfume 0.1 0.1 0.1 0.1 0.1 0.1
    Stability ×
    Texture (Spreadability on skin) Δ × Δ
    (stickiness) Δ × Δ ×
    (lightness) × Δ ×
    Skin improving effect (skin resilience) × Δ ×
    (skin moisturizing) Δ Δ ×
  • Tables 1 and 2 show that Examples 1 to 7 according to the invention are excellent in stability, texture, and skin improving effect. In contrast, not all of stability, texture, and skin improving effect are satisfactory with respect to Comparative Examples 1 to 6, which do not satisfy the requirements of the invention.
    Specifically, Comparative Examples 1 to 3 and 6 lack any of the ingredients (A) , (B) , (C) , and (D) . Comparative Example 1 not containing the ingredient (A) is sticky and lacks a skin moisturizing effect. Comparative Example 2 not containing the ingredient (B) particularly has a problem with stability. Comparative Example 3 not containing the ingredient (C) is significantly inferior in texture such as spreadability on skin, stickiness, or lightness. Comparative Example 6 not containing the ingredient (D) does not produce a skin improving effect such as a skin moisturizing effect.
  • Comparative Example 4 containing another thickener (carboxyvinyl polymer) instead of the ingredient (B) is insufficient in texture with respect to stickiness, lightness, etc. and insufficient in skin improving effect. Comparative Example 5 containing squalane with an IOB of 0 instead of the ingredient (C) is sticky and lacks spreadability on skin and lightness, although it makes the skin resilient and moisturized.
  • Hereinafter, other examples of the invention are shown.
  • Example 8: Anti-Aging Cream
  • (Ingredients) % by mass
    (1) Liquid paraffin 2.0
    (2) Decamethylcyclopentanesiloxane 5.0
    (3) Isodecyl benzoate (IOB=0.23) [ingredient (C)] 5.0
    (4) Polyoxyethylene (21) stearyl ether 2.0
    (5) Polyoxyethylene (2) stearyl ether 0.5
    (6) Cetyl alcohol 2.5
    (7) Batyl alcohol 2.0
    (8) Perfume 0.1
    (9) Ion-exchanged water q.s.
    (10) Dipropylene glycol 3.0
    (11) Glycerin [ingredient (D)] 11.0
    (12) Paraben 0.15
    (13) Ethanol 3.0
    (14) Potassium hydroxide 0.4
    (15) Dimethylacrylamide/sodium
    2-acrylamido-2-methylpropanesulfonate crosspolymer [ingredient (B)] 0.8
    (Trade name: SU-POLYMER G-1, manufactured by TOHO Chemical Industry Co., Ltd.)
    (16) Citric acid 0.01
    (17) Sodium citrate 0.09
    (18) D-hydroxyproline [ingredient (A)] 2.0
  • <Preparation Process>
  • Ingredients (1) to (8) were uniformly mixed and dissolved at 70°C (oil phase) . On the other hand, ingredients (9) to (18) were uniformly mixed and dissolved at 70°C (aqueous phase) . While the oil phase was gradually added to the aqueous phase kept at 70°C, the mixture was emulsified with a homomixer. After the emulsification was completed, the emulsion was rapidly cooled to 40°C or less to give the desired anti-aging cream.
  • <Product Properties>
  • The resulting cream was evaluated in the same manner as described above for Examples 1 to 7. As a result, the cream had good texture (the evaluation was ⊙ with respect to all of skin spreadability, stickiness, and lightness) , a moisturizing effect, light spreadability, and a moist feeling with lightness when applied to the skin, and also had good stability (the stability was evaluated "O").
  • Example 9: O/W Emulsion-Type Sunscreen
  • (Ingredients) % by mass
    (1) Octyl p-methoxycinnamate 6.0
    (2) Glyceryloctyl di-p-methoxycinnamate 2.0
    (3) 4-tert-butyl-4'-methoxybenzoylmethane 2.0
    (4) Pentaerythritol tetra(octanoate/p-methoxycinnamate) 3.0
    (5) Tripropylene glycol dineopentanoate (IOB=0.52) [ingredient (C)] 5.0
    (6) Dimethylpolysiloxane (20 mPa·s) 3.0
    (7) Petrolatum 0.5
    (8) PEG (40) glyceryl isostearate 1.2
    (9) Sorbitan tristearate 0.25
    (10) Ion-exchanged water balance
    (11) 1,3-butylene glycol 3.0
    (12) Glycerin [ingredient (D)] 5.0
    (13) Ethanol 3.0
    (14) Acrylamide/sodium 2-acrylamido-2-methylpropanesulfonate (40% in active content) [ingredient (B)] 1.0 (0.4)
    (Trade name: SEPIGEL 305, manufactured by SEPIC)
    (15) Perfume 0.1
    (16) D-methionine [ingredient (A)] 0.5
  • <Preparation Process>
  • Ingredients (1) to (9) were uniformly mixed and dissolved at 70°C (oil phase). On the other hand, ingredients (10) to (16) were uniformly mixed and dissolved at 70°C (aqueous phase) . While the oil phase was gradually added to the aqueous phase kept at 70°C, the mixture was emulsified with a homomixer. After the emulsification was completed, the emulsion was rapidly cooled to 40°C or less to give the desired O/W emulsion type sunscreen.
  • <Product Properties>
  • The resulting sunscreen was evaluated in the same manner as Examples 1 to 7. As a result, the sunscreen had good texture (the evaluation was ⊙ with respect to all of skin spreadability, stickiness, and lightness), a moisturizing effect, light spreadability, and a moist feeling with lightness when applied to the skin, and also had good stability (the stability was evaluated "O") .
  • Example 10: Whitening Cream
  • (Ingredients) % by mass
    (1) Hydrogenated polyisobutene 2.0
    (2) Isododecane 6.0
    (3) Isodecyl benzoate (IOB=0.23) [ingredient (C)] 3.0
    (4) Polyoxyethylene (30) behenyl ether 3.0
    (5) Cetyl alcohol 2.5
    (6) Batyl alcohol 2.5
    (7) Perfume 0.1
    (8) Ion-exchanged water balance
    (9) 1,3-butylene glycol 3.0
    (10) Glycerin [ingredient (D)] 6.0
    (11) Arbutin 5.0
    (12) Magnesium ascorbate phosphate 1.0
    (13) Paraben 0.15
    (14) Ethanol 3.0
    (15) Potassium hydroxide q.s.
    (16) (Hydroxyethyl acrylate/sodium 2-acrylamido-2-methylpropanesulfonate) copolymer (37.5% in active content) [ingredient (B)] 1.3 (0.49)
    (trade name: SIMULGEL NS, manufactured by SEPIC)
    (17) Citric acid 0.01
    (18) Sodium citrate 0.09
    (19) D-serine [ingredient (A)] 2.5
  • <Preparation Process>
  • Ingredients (1) to (7) were uniformly mixed and dissolved at 70°C (oil phase). On the other hand, ingredients (8) to (19) were uniformly mixed and dissolved at 70°C (aqueous phase). While the oil phase was gradually added to the aqueous phase kept at 70°C, the mixture was emulsified with a homomixer. After the emulsification was completed, the emulsion was rapidly cooled to 40°C or less to give the desired whitening cream.
  • <Product Properties>
  • The resulting whitening cream was evaluated in the same manner as Examples 1 to 7. As a result, the cream had good texture (the evaluation was ⊙ with respect to all of skin spreadability, stickiness, and lightness), a moisturizing effect, light spreadability, and a moist feeling with lightness when applied to the skin, and also had good stability (the stability was evaluated "O").
  • Example 11: Whitening Cream
  • (Ingredients) % by mass
    (1) Liquid paraffin 2.0
    (2) Dimethysilicone (1.5 mPa·s) 6.0
    (3) Isononyl isononanoate (IOB=0.2) [ingredient (C)] 3.0
    (4) Polyoxyethylene (20) sorbitan monostearate 3.0
    (5) Sorbitan trioleate 0.3
    (6) Cetyl alcohol 2.5
    (7) Batyl alcohol 1.0
    (8) Perfume 0.1
    (9) 1,3-butylene glycol 5.0
    (10) Glycerin [ingredient (D)] 7.0
    (11) Ion-exchanged water balance
    (12) Trimethylglycine 0.1
    (13) Potassium 4-methoxysalicylate 2.0
    (14) Phenoxyethanol 0.2
    (15) Sodium hydroxide q.s.
    (16) (Hydroxyethyl acrylate/sodium 2-acrylamido-2-methylpropanesulfonate) copolymer [ingredient (B)] 1.5
    (trade name: SEPINOV EMT 10, manufactured by SEPIC)
    (17) Citric acid 0.02
    (18) Sodium citrate 0.08
    (19) D-glutamic acid [ingredient (A)] 0.5
    (20) D-aspartic acid [ingredient (A)] 1.0
  • <Preparation Process>
  • Ingredients (1) to (8) were uniformly mixed and dissolved at 70°C (oil phase). On the other hand, ingredients (9) to (20) were uniformly mixed and dissolved at 70°C (aqueous phase). While the oil phase was gradually added to the aqueous phase kept at 70°C, the mixture was emulsified with a homomixer. After the emulsification was completed, the emulsion was rapidly cooled to 40°C or less to give the desired whitening cream.
  • <Product Properties>
  • The resulting whitening cream was evaluated in the same manner as Examples 1 to 7. As a result, the cream had good texture (the evaluation was ⊙ with respect to all of skin spreadability, stickiness, and lightness), a moisturizing effect, light spreadability, and a moist feeling with lightness when applied to the skin, and also had good stability (the stability was evaluated "O").

Claims (5)

  1. An oil-in-water type emulsion skin cosmetic composition, comprising:
    (A) a D-amino acid or a derivative or salt thereof;
    (B) a homopolymer, a copolymer, or a crosspolymer comprising, as a constituent unit, one or more selected from 2-acrylamido-2-methylpropanesulfonic acid, acrylic acid, and derivatives thereof;
    (C) an ester oil with an IOB value of 0.2 to 0.6; and
    (D) glycerin.
  2. The oil-in-water emulsion skin cosmetic composition according to claim 1,
    wherein the D-amino acid is selected from the group consisting of D-glutamic acid, D-alanine, D-methionine, D-hydroxyproline, D-aspartic acid, D-cysteine, D-serine, and D-proline.
  3. The oil-in-water emulsion skin cosmetic composition according to claim 1 or 2, which contains
    0.1 to 5.0% by mass of the ingredient (A),
    0.1 to 2.0% by mass of the ingredient (B),
    1.0 to 15.0% by mass of the ingredient (C), and
    5.0 to 15.0% by mass of the ingredient (D) based on the total amount of the cosmetic composition.
  4. The oil-in-water emulsion skin cosmetic composition according to any one of claims 1 to 3,
    wherein the ingredient (B) is one or more selected from a vinylpyrrolidone/2-acrylamido-2-methylpropanesulfonic acid (salt) copolymer, a dimethylacrylamide/2-acrylamido-2-methylpropanesulfonic acid (salt) copolymer, an acrylamide/acrylic acid/2-acrylamido-2-methylpropanesulfonic acid (salt) copolymer, a mixture of polyacrylamide and polyacrylic acid (salt), a sodium acrylate/2-acrylamido-2-methylpropanesulfonic acid (salt) copolymer, an acrylamide/acrylic acid (salt) copolymer, a homopolymer of 2-acrylamido-2-methylpropanesulfonic acid (salt), and a vinylformamide/2-acrylamido-2-methylpropanesulfonic acid (salt) copolymer.
  5. The oil-in-water emulsion skin cosmetic composition according to any one of claims 1 to 4,
    wherein the ingredient (C) is one or more selected from tripropylene glycol dineopentanoate (IOB=0.52), isodecyl benzoate (IOB=0.23), propylene glycol dicaprylate (IOB=0.32), isononyl isononanoate (IOB=0.2), cetyl 2-ethylhexanoate (IOB=0.52), glyceryl tri-2-ethylhexanoate (IOB=0.36), isodecyl neopentanoate (IOB=0.22), 2-ethylhexyl 2-ethylhexanoate (IOB=0.2), pentaerythritol tetra-2-ethylhexanoate (IOB=0.35), di-2-ethylhexyl succinate (IOB=0.32), and 2-ethylhexyl isononanoate (IOB=0.2).
EP11795586.4A 2010-06-17 2011-06-06 Oil-in-water type emulsion skin cosmetic Active EP2583663B1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP2010138388 2010-06-17
JP2011125099A JP5689026B2 (en) 2010-06-17 2011-06-03 Oil-in-water emulsified skin cosmetic
PCT/JP2011/062892 WO2011158678A1 (en) 2010-06-17 2011-06-06 Oil-in-water type emulsion skin cosmetic

Publications (3)

Publication Number Publication Date
EP2583663A1 true EP2583663A1 (en) 2013-04-24
EP2583663A4 EP2583663A4 (en) 2015-08-19
EP2583663B1 EP2583663B1 (en) 2019-04-03

Family

ID=45348084

Family Applications (1)

Application Number Title Priority Date Filing Date
EP11795586.4A Active EP2583663B1 (en) 2010-06-17 2011-06-06 Oil-in-water type emulsion skin cosmetic

Country Status (8)

Country Link
US (1) US8697750B2 (en)
EP (1) EP2583663B1 (en)
JP (1) JP5689026B2 (en)
KR (1) KR101692801B1 (en)
CN (1) CN102946849B (en)
ES (1) ES2726452T3 (en)
TW (1) TWI495483B (en)
WO (1) WO2011158678A1 (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2762128A1 (en) * 2011-09-30 2014-08-06 Shiseido Company, Ltd. Oil-in-water-type emulsion cosmetic
WO2015164290A1 (en) * 2014-04-23 2015-10-29 The Procter & Gamble Company Cosmetic compositions having reduced irritation
WO2018096224A1 (en) * 2016-11-25 2018-05-31 Urgo Recherche Innovation Et Developpement Film-forming composition
RU2666253C2 (en) * 2013-07-12 2018-09-06 Пьер Фабр Дермо-Косметик Cosmetic composition comprising a ternary lipid association for controlling dryness of the skin
EP3533440A4 (en) * 2016-10-31 2020-06-17 Shiseido Co., Ltd. Oil-in-water type dermatological composition for external use

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2012097149A1 (en) 2011-01-14 2012-07-19 Dow Agrosciences Llc Agricultural compositions comprising oil-in-water emulsions
US10281267B2 (en) 2014-11-10 2019-05-07 Shiseido Company, Ltd. Method for evaluating flow of skin, method for examining skin glow improvers, and skin glow improver
WO2018056989A1 (en) 2016-09-22 2018-03-29 Colgate-Palmolive Company Personal care gel and method
JP7172985B2 (en) * 2017-03-24 2022-11-16 味の素株式会社 whitening agent
CN108670890B (en) * 2018-07-17 2020-06-26 广州澳希亚实业有限公司 Organic sunscreen composition and application thereof
EP3903762A4 (en) * 2018-12-28 2022-10-26 Shiseido Company, Ltd. Retinol-containing oil-in-water type emulsified cosmetic material
FR3142086A1 (en) * 2022-11-17 2024-05-24 L'oreal COMPOSITION COMPRISING A LARGE QUANTITY OF POLYOL
WO2024075555A1 (en) * 2022-10-04 2024-04-11 L'oreal Composition comprising large amount of polyol

Family Cites Families (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4482537A (en) * 1983-09-19 1984-11-13 Charles Of The Ritz Group Ltd. Skin conditioning composition
JPS6467685A (en) 1987-09-09 1989-03-14 Hitachi Ltd Wiring method for wiring length designation
US5061721A (en) * 1989-03-15 1991-10-29 G. D. Searle & Co. Composition containing d-cycloserine and d-alanine for memory and learning enhancement or treatment of a cognitive or psychotic disorder
FR2750327B1 (en) 1996-06-28 1998-08-14 Oreal COMPOSITION FOR TOPICAL USE IN THE FORM OF OIL-IN-WATER EMULSION WITHOUT SURFACTANT CONTAINING A POLY (2-ACRYLAMIDO 2-METHYLPROPANE SULFONIC) CROSSLINKED AND NEUTRALIZED
JPH1160436A (en) * 1997-08-20 1999-03-02 Shiseido Co Ltd Cosmetic for improving chapped skin
JP3834960B2 (en) 1997-10-14 2006-10-18 味の素株式会社 Method for producing D-amino acid
JPH11246329A (en) 1998-02-27 1999-09-14 Shiseido Co Ltd Skin preparation for external use
JP3589283B2 (en) 1998-12-25 2004-11-17 ライオン株式会社 Hair cosmetics
JP3681154B2 (en) 1999-10-14 2005-08-10 株式会社資生堂 Water-soluble thickener and cosmetics containing the same
JP2002356416A (en) 2001-05-30 2002-12-13 Shiseido Co Ltd Water-in-oil type emulsified cosmetic for preventing rough skin
JP3682419B2 (en) * 2001-06-19 2005-08-10 株式会社ノエビア Topical skin preparation
JP4838537B2 (en) * 2005-05-25 2011-12-14 株式会社 資生堂 Inadequate keratinization inhibitor, pore-reducing agent, skin roughening preventive / improving agent, and composition for external use on skin
JP2008001654A (en) * 2006-06-23 2008-01-10 Ajinomoto Co Inc External preparation for skin
JP4968722B2 (en) * 2006-09-22 2012-07-04 株式会社 資生堂 Oil-in-water emulsified skin cosmetic
KR101392380B1 (en) * 2007-02-21 2014-05-07 주식회사 엘지생활건강 Powder detergent granule containing acidic water-soluble polymer and manufacturing method thereof
FR2916351B1 (en) * 2007-05-22 2012-12-07 Galderma Res & Dev PHARMACEUTICAL COMPOSITION COMPRISING AT LEAST TWO COMPOUNDS SELECTED BY PYRROLIDONE-5-CARBOXYLIC ACID, CITRULLINE, ARGININE AND ASPARAGINE AND THEIR USE IN THE TREATMENT OF ATOPIC DERMATITIS
CN101925353A (en) * 2008-01-21 2010-12-22 株式会社资生堂 VEGFC production promoter
JP5277011B2 (en) * 2008-02-13 2013-08-28 株式会社 資生堂 Oil-in-water emulsified cloudy skin cosmetic
JP5180633B2 (en) * 2008-03-14 2013-04-10 花王株式会社 Skin cleanser
JP2009298752A (en) * 2008-06-17 2009-12-24 Shiseido Co Ltd Skin care preparation composition for external use
DE102008047944A1 (en) * 2008-09-18 2009-06-25 Henkel Ag & Co. Kgaa Cosmetic or dermatological composition, useful e.g. for cosmetic tanning of human hair and for coloring of the hair, comprises an alpha-melanocyte-stimulating hormone analogue and acetyl-methionyl-arginine-ethyl ester
US8926996B2 (en) * 2008-12-03 2015-01-06 Shiseido Company, Ltd. Oil-in-water cosmetics

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2762128A1 (en) * 2011-09-30 2014-08-06 Shiseido Company, Ltd. Oil-in-water-type emulsion cosmetic
EP2762128A4 (en) * 2011-09-30 2015-04-29 Shiseido Co Ltd Oil-in-water-type emulsion cosmetic
US9956148B2 (en) 2011-09-30 2018-05-01 Shiseido Company, Ltd. Oil-in-water-type emulsion cosmetic
RU2666253C2 (en) * 2013-07-12 2018-09-06 Пьер Фабр Дермо-Косметик Cosmetic composition comprising a ternary lipid association for controlling dryness of the skin
WO2015164290A1 (en) * 2014-04-23 2015-10-29 The Procter & Gamble Company Cosmetic compositions having reduced irritation
US9480634B2 (en) 2014-04-23 2016-11-01 The Procter & Gamble Company Cosmetic compositions
EP3533440A4 (en) * 2016-10-31 2020-06-17 Shiseido Co., Ltd. Oil-in-water type dermatological composition for external use
US12059489B2 (en) 2016-10-31 2024-08-13 Shiseido Company, Ltd. Oil-in-water type dermatological composition for external use
WO2018096224A1 (en) * 2016-11-25 2018-05-31 Urgo Recherche Innovation Et Developpement Film-forming composition

Also Published As

Publication number Publication date
KR20130109949A (en) 2013-10-08
US20130079410A1 (en) 2013-03-28
WO2011158678A1 (en) 2011-12-22
EP2583663A4 (en) 2015-08-19
US8697750B2 (en) 2014-04-15
CN102946849A (en) 2013-02-27
EP2583663B1 (en) 2019-04-03
TWI495483B (en) 2015-08-11
TW201208710A (en) 2012-03-01
JP5689026B2 (en) 2015-03-25
JP2012020988A (en) 2012-02-02
KR101692801B1 (en) 2017-01-05
ES2726452T3 (en) 2019-10-04
CN102946849B (en) 2015-04-01

Similar Documents

Publication Publication Date Title
US8697750B2 (en) Oil-in-water type emulsion skin cosmetic
JP4679350B2 (en) Oil-in-water emulsified skin cosmetic
EP2786745B1 (en) Aqueous cosmetic preparation for skin
EP2740462B1 (en) Oil-in-water-type emulsion cosmetic
JP4968722B2 (en) Oil-in-water emulsified skin cosmetic
EP2301522B1 (en) Water-in-oil emulsion-type cosmetic preparation
US8980234B2 (en) Cosmetic composition comprising an ascorbic acid or salicylic acid compound
KR20060130215A (en) Oil-in-water emulsified composition, and external preparation for skin and cosmetics using the composition
US20200345596A1 (en) Skin-tightening composition
JP4827433B2 (en) Oil-in-water emulsified skin cosmetic
WO2012017733A1 (en) Skin cosmetic
ES2351381T3 (en) COSMETIC COMPOSITION THAT INCLUDES AN ASCORBIC ACID COMPOUND OR A SALICYLIC ACID COMPOUND.
JP5506106B2 (en) Oil-in-water emulsified skin cosmetic
JP2013063935A (en) Oil-in-water emulsion skin cosmetic
JP5398813B2 (en) Aqueous skin cosmetics
JP5088979B1 (en) Oil-in-water emulsified skin cosmetic
JP2007145719A (en) Emulsified type external preparation for skin
JP2016084323A (en) Cosmetics and skin condition improving method
JP2021161112A (en) Composition
JP2016204317A (en) Skin external preparation
JP2006143686A (en) Emulsion composition

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 20130108

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

DAX Request for extension of the european patent (deleted)
RA4 Supplementary search report drawn up and despatched (corrected)

Effective date: 20150717

RIC1 Information provided on ipc code assigned before grant

Ipc: A61K 8/81 20060101ALI20150713BHEP

Ipc: A61K 8/37 20060101ALI20150713BHEP

Ipc: A61Q 19/00 20060101ALI20150713BHEP

Ipc: A61K 8/06 20060101ALI20150713BHEP

Ipc: A61K 8/44 20060101AFI20150713BHEP

Ipc: A61K 8/34 20060101ALI20150713BHEP

Ipc: A61Q 19/02 20060101ALI20150713BHEP

Ipc: A61Q 17/04 20060101ALI20150713BHEP

17Q First examination report despatched

Effective date: 20160926

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: EXAMINATION IS IN PROGRESS

GRAP Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOSNIGR1

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: GRANT OF PATENT IS INTENDED

INTG Intention to grant announced

Effective date: 20181008

GRAS Grant fee paid

Free format text: ORIGINAL CODE: EPIDOSNIGR3

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE PATENT HAS BEEN GRANTED

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

REG Reference to a national code

Ref country code: GB

Ref legal event code: FG4D

REG Reference to a national code

Ref country code: CH

Ref legal event code: EP

Ref country code: AT

Ref legal event code: REF

Ref document number: 1114855

Country of ref document: AT

Kind code of ref document: T

Effective date: 20190415

REG Reference to a national code

Ref country code: IE

Ref legal event code: FG4D

REG Reference to a national code

Ref country code: DE

Ref legal event code: R096

Ref document number: 602011057796

Country of ref document: DE

REG Reference to a national code

Ref country code: NL

Ref legal event code: MP

Effective date: 20190403

REG Reference to a national code

Ref country code: LT

Ref legal event code: MG4D

REG Reference to a national code

Ref country code: AT

Ref legal event code: MK05

Ref document number: 1114855

Country of ref document: AT

Kind code of ref document: T

Effective date: 20190403

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: NL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190403

REG Reference to a national code

Ref country code: ES

Ref legal event code: FG2A

Ref document number: 2726452

Country of ref document: ES

Kind code of ref document: T3

Effective date: 20191004

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: AL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190403

Ref country code: CZ

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190403

Ref country code: PT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190803

Ref country code: NO

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190703

Ref country code: LT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190403

Ref country code: HR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190403

Ref country code: SE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190403

Ref country code: FI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190403

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: GB

Payment date: 20190624

Year of fee payment: 9

Ref country code: IT

Payment date: 20190726

Year of fee payment: 9

Ref country code: ES

Payment date: 20190723

Year of fee payment: 9

Ref country code: DE

Payment date: 20190628

Year of fee payment: 9

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: LV

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190403

Ref country code: RS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190403

Ref country code: BG

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190703

Ref country code: GR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190704

Ref country code: PL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190403

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: IS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190803

Ref country code: AT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190403

REG Reference to a national code

Ref country code: DE

Ref legal event code: R097

Ref document number: 602011057796

Country of ref document: DE

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MC

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190403

Ref country code: SK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190403

Ref country code: EE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190403

Ref country code: DK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190403

Ref country code: RO

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190403

REG Reference to a national code

Ref country code: CH

Ref legal event code: PL

PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SM

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190403

26N No opposition filed

Effective date: 20200106

REG Reference to a national code

Ref country code: BE

Ref legal event code: MM

Effective date: 20190630

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: TR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190403

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: IE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20190606

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: CH

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20190630

Ref country code: SI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190403

Ref country code: BE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20190630

Ref country code: LU

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20190606

Ref country code: LI

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20190630

REG Reference to a national code

Ref country code: DE

Ref legal event code: R119

Ref document number: 602011057796

Country of ref document: DE

GBPC Gb: european patent ceased through non-payment of renewal fee

Effective date: 20200606

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: GB

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20200606

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: CY

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190403

Ref country code: DE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20210101

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190403

Ref country code: HU

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT; INVALID AB INITIO

Effective date: 20110606

REG Reference to a national code

Ref country code: ES

Ref legal event code: FD2A

Effective date: 20211026

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: IT

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20200606

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: ES

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20200607

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190403

P01 Opt-out of the competence of the unified patent court (upc) registered

Effective date: 20230613

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: FR

Payment date: 20240521

Year of fee payment: 14